BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

286 related articles for article (PubMed ID: 8487285)

  • 1. Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
    Trautmann U; Pfeiffer RA; Seufert-Satomi U; Tietze HU
    J Med Genet; 1993 Apr; 30(4):330-1. PubMed ID: 8487285
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 16q21 is critical for 16q deletion syndrome.
    Naritomi K; Shiroma N; Izumikawa Y; Sameshima K; Ohdo S; Hirayama K
    Clin Genet; 1988 May; 33(5):372-5. PubMed ID: 3378367
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo 3q/7q translocation and associated interstitial 7q35 deletion.
    Fryns JP; Kleczkowska A; van den Berghe H
    Clin Genet; 1988 Jan; 33(1):60-2. PubMed ID: 3342549
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boy.
    Schuffenhauer S; Callen DF; Seidel H; Shen Y; Lederer G; Murken J
    Clin Genet; 1992 Nov; 42(5):246-50. PubMed ID: 1486702
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inverted tandem duplication generates a duplication deficiency of chromosome 8p.
    Dill FJ; Schertzer M; Sandercock J; Tischler B; Wood S
    Clin Genet; 1987 Aug; 32(2):109-13. PubMed ID: 2888552
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
    Silengo MC; Davi GF; Bianco R; Biagioli M; Guala A; Franceschini P; Novelli G
    Clin Genet; 1984 Jun; 25(6):549-52. PubMed ID: 6587954
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
    Stoll C; Levy J; Roth MP
    J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of de novo interstitial deletion 3q.
    Okada N; Hasegawa T; Osawa M; Fukuyama Y
    J Med Genet; 1987 May; 24(5):305-8. PubMed ID: 3585947
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A; Cain R; Howell R
    Hum Genet; 1980; 53(3):305-7. PubMed ID: 7372333
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Three cases of 16q duplication.
    Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV
    J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771
    [No Abstract]   [Full Text] [Related]  

  • 11. Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22).
    Ohdo S; Madokoro H; Hayakawa K
    J Med Genet; 1982 Dec; 19(6):479. PubMed ID: 7154050
    [No Abstract]   [Full Text] [Related]  

  • 12. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).
    Fryns JP; Casaer P; Van den Berghe H
    Hum Genet; 1979 Jan; 46(2):237-41. PubMed ID: 422207
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A unique de novo interstitial deletion del(17)(q21.3q23) in a phenotypically abnormal infant.
    Park JP; Moeschler JB; Berg SZ; Bauer RM; Wurster-Hill DH
    Clin Genet; 1992 Jan; 41(1):54-6. PubMed ID: 1633649
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Two siblings with interstitial deletion of chromosome 14 [46 XX, del (14) (q12 q13.3)]].
    Kodama M; Kai Y; Sugino S; Inokuchi N; Miike T
    No To Hattatsu; 1990 Jan; 22(1):61-5. PubMed ID: 2294952
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interstitial deletion of chromosome 13: prognosis and adult phenotype.
    Dean JC; Simpson S; Couzin DA; Stephen GS
    J Med Genet; 1991 Aug; 28(8):533-5. PubMed ID: 1920369
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial deletion of the short arm of chromosome 4.
    Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A de novo interstitial deletion of 15(q21.2q22.1) in a moderately retarded adult male.
    Martin F; Platt J; Tawn EJ; Burn J
    J Med Genet; 1990 Oct; 27(10):637-9. PubMed ID: 2246774
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recurrent de novo interstitial deletion of 16q in two mentally retarded sisters.
    Hoo JJ; Lowry RB; Lin CC; Haslam RH
    Clin Genet; 1985 Apr; 27(4):420-5. PubMed ID: 3995793
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interstitial deletion and ring chromosome derived from 16q.
    Krauss CM; Caldwell D; Atkins L
    J Med Genet; 1987 May; 24(5):308-12. PubMed ID: 3585948
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High resolution pattern of an inverted duplication (15).
    Hoo JJ
    Clin Genet; 1986 Mar; 29(3):241-5. PubMed ID: 3457663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.